## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
β¦ LIBER β¦
Isolation of a New Caryophyllane Ester from Lactarius subumbonatus: Conformational Analysis and Absolute Configuration
β Scribed by Marco Clericuzio; Lucio Toma; Giovanni Vidari
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 203 KB
- Volume
- 1999
- Category
- Article
- ISSN
- 1434-193X
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β¦ Synopsis
The absolute configuration of the sesquiterpene moiety has been established by theoretical Circular Dichroism sesquiterpene alcohol esterified by the unusual fatty acid (S)-(+)-6-hydroxystearic acid, has been isolated from the fruiting calculations (De Voe coupled oscillators theory) and that of the fatty acid by NMR studies of the (R)-2-methoxy-2-bodies of the Basidiomycete Lactarius subumbonatus. Both NMR data and AM1 calculations indicate that the naphthylacetic acid (2-NMA) ester. caryophyllene macrocyclic ring adopts a Ξ²Ξ² conformation.
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